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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1763998Generated: November 1, 2026

Bromhydrol → HCID 70528502, compound

https://huagongshe.com/reaction/1763998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromhydrolHCID 166749—
ReactantHCID 70528163HCID 70528163—
SolventDichloromethaneHCID 6344—
ProductHCID 70528502HCID 7052850233.3%

Reaction Steps

A solution of methyl 2-methyl-2,3-methylene-6-(2-phenoxyacetamido)-penam-3-carboxylate (2.1 g.) in dried dichloromethane (11 ml.) was dropwise added over 8 minutes at -10° C. to a solution of aluminum bromide (2.32 g.) in dried dichloromethane (23 ml.) and the reaction temperature was gradually elevated to room temperature, after which the mixture was stirred for 4.4 hours at room temperature. After the reaction, the reaction mixture was poured into ice-water (150 ml.) and the dichloromethane layer was separated, after which the aqueous layer was once extracted with chloroform. The combined dichloromethane and chloroform extract was washed in turn with water, 2% hydrochloric acid, water, a dilute sodium bicarbonate aqueous solution and water, and then dried over magnesium sulfate. After the solvent was distilled off, the obtained yellow oil was purified by column chromatography on silica gel (15 g.) using chloroform as developing solvent to give orange oil of methyl 2-methyl-7-(2-phenoxyacetamido)-3-cephem-4-carboxylate (0.7 g.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04113940
Source datasetuspto-grants-1978_09
ORD IDord-f1c98953b8274a2ebb0e891915747c88
Source noteuspto-grants-1978_09